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PD-1/PD-L1在非小细胞肺癌的治疗研究进展 被引量:10

Research progress of PD-1/PD-L1 in the treatment of non-small cell lung cancer
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摘要 有限的干预手段使得肺癌患者面临着欠佳的预后。近年来免疫治疗成为了继手术、放疗、化疗等治疗后非小细胞肺癌(non-smallcell lung cancer,NSCLC)的新型研究方向。以程序性死亡分子1(programmed death-1,PD-1)/程序性死亡分子1配体(programmed death-1 ligand,PD-L1)为代表的免疫检查点在肿瘤的发生发展中起到重要作用,证实了其抑制剂抗PD-1单抗在晚期非小细胞肺癌患者生存的相关性,以及PD-L1作为疗效预测的生物标记物的潜力。目前,nivolumab和pembrolizumab已经开启了在非小细胞肺癌治疗上的先河。FDA于2015批准了上述两种免疫抑制剂在非小细胞肺癌二线治疗中的临床应用。本文对PD-1/PD-L1信号通路、抗PD-1单抗在非小细胞肺癌中的作用机制、临床现状及展望进行综述。 Limited therapies lead to an undesirable prognosis to patients with lung cancer. In recent years, immune therapy has become a new direction in the treatment of non-small cell lung cancer in addition to surgery, radiotherapy, chemotherapy and so on. The immune checkpoints represented by programmed death-1 (PD-1) and programmed death-1 ligand (PD-L1) have a significant influence on the development of cancer, indicating the relationship between the inhibitors like anti-PD-1/PD-L1 monoclonal antibody and survival, and the potential to PD-L1 as biomarker for curative effect. At present, nivolumab and perbrolizumab have created another way focusing on non-small cell lung cancer. In 2015, the FDA approved the two aboved-mentioned immune inhibitors as the second-line treatment for patients suffering non-small cell lung cancer. In this article, we summarized the signal pathway of PD-1/PD-L1, and action mechanism of anti-PD-1 monoclonal antibody in non-small cell lung cancer, as well as its clinical current status and future direction.
作者 蹇丹 陈晓品
出处 《中国新药杂志》 CAS CSCD 北大核心 2016年第17期1967-1972,共6页 Chinese Journal of New Drugs
关键词 PD-1/PD-L 抗PD-1单抗 非小细胞肺癌 免疫检查点 免疫逃逸 PD-1/PD-L1 anti-PD-1 monoclonal antibody non-small cell lung cancer immunecheckpoints immune escape
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  • 1FERLAY J, SOERJOMATARAM I,ERVIK M, et al. GLOBO-CAN 2012 VI. 0,cancer incidence and mortality worldwide:IAR.C cancer base No. 11 [ EB/OL ]. Lyon France : InternationalAgency for Research on Cancer,2013 [2014 - 10 -08]. http : //globocan. iara. fr. 被引量:1
  • 2GUO J, SI L, KONG Y , et al. A phase II open label single-armtrial of imatinib mesylate in patients with metastatic melanomaharboring c-Kit mutation or amplification [ J ] . J Clin Oncol,2011 , 29(21) : 2904 -2909. 被引量:1
  • 3CHAPMAN PB, HAUSCHILD A, ROBERT C, et al. Improvedsurvival with vemurafenib in melanoma with BRAF V600E muta-tion[J], N Engl J Med, 2011,364(26) :2507 -2516. 被引量:1
  • 4HAUSCHILD A, GROB JJ, DEMIDOV LV, et al. Dabrafenib infi/?y4F-mutated metastatic melanoma : a multicentre, open-label,phase 3 randomised controlled trial [ J ]. Lancet, 2012 , 380(9839) : 358 -365. 被引量:1
  • 5FLAHERTY KT, ROBERT C, HERSEY P, et al. Improved sur-vival with MEK inhibition in /'-mutated melanoma[ J]. /V En-gl J Med, 2012,367(2) :107 -114. 被引量:1
  • 6HODI FS, O'DAY SJ, MCDERMOTT DF, et al. improved sur-vival with ipilimumab in patients with metastatic melanoma [ J ].N Engl J Med, 2010,363(8) :711 -723. 被引量:1
  • 7HAMID 0,ROBERT C , DAUD A, et al. Safety and tumor re-sponses with lambrolizumab ( anti-PD-1 ) in melanoma [ J ]. NEngl J Med, 2013,369(2) :134 - 144. 被引量:1
  • 8郭军.重组人血管内皮抑素联合DT1C对比DTIC单药一线治疗晚期黑色素瘤患者的随机、双盲、多中心n期临床研究[N].中国医学论坛报,2012 -07 - 10. 被引量:1
  • 9PLATZ A, EGYHAZI S, RINGBORG U, et al. Human cutane-ous melanoma, a review of NRAS and BRAF mutation frequenciesin relation to histogenetic subclass and body site[ J ] . Mol Oncol,2008,1(4) : 395 -405. 被引量:1
  • 10CURTIN JA,FRIDLYAND J, KAGESHITA T, et al. Distinctsets of genetic alterations in melanoma [ J ] . N Engl J Med,2005, 353(20) : 2135 -2147. 被引量:1

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